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Proc Natl Acad Sci U S A. 2010 Oct 19;107(42):17962-7. doi: 10.1073/pnas.1006687107. Epub 2010 Oct 4.

Structures of aminoacylase 3 in complex with acetylated substrates.

Author information

1
Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.

Abstract

Trichloroethylene (TCE) is one of the most widespread environmental contaminants, which is metabolized to N-acetyl-S-1,2-dichlorovinyl-L-cysteine (NA-DCVC) before being excreted in the urine. Alternatively, NA-DCVC can be deacetylated by aminoacylase 3 (AA3), an enzyme that is highly expressed in the kidney, liver, and brain. NA-DCVC deacetylation initiates the transformation into toxic products that ultimately causes acute renal failure. AA3 inhibition is therefore a target of interest to prevent TCE induced nephrotoxicity. Here we report the crystal structure of recombinant mouse AA3 (mAA3) in the presence of its acetate byproduct and two substrates: N(α)-acetyl-L-tyrosine and NA-DCVC. These structures, in conjunction with biochemical data, indicated that AA3 mediates substrate specificity through van der Waals interactions providing a dynamic interaction interface, which facilitates a diverse range of substrates.

PMID:
20921362
PMCID:
PMC2964198
DOI:
10.1073/pnas.1006687107
[Indexed for MEDLINE]
Free PMC Article

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